- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06674174
Effect of Lower Limb Resistance Versus Endurance Training in Smokers
November 3, 2024 updated by: Riphah International University
Effects of Lower Limb Resistance Versus Endurance Training on Pulmonary Function in Smokers With Shortness of Breath
Patients was selected based on inclusion and exclusion criteria.
Experimental group was treated with Resistance training while control group received endurance training.
Data was collected by spirometry and International Physical activity questionnaire readings was recorded in every session for baseline, 3rd week and 6thweeks.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Experimental group will receive lower limb strength training and control group will receive endurance training.
Both groups will receive treatment for three days a week and each session will be given according to FITT formula.
Measurement will be recorder pre-treatment and post treatment of both groups at baseline, third , and 6 th week.
Study Type
Interventional
Enrollment (Actual)
60
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Dera Ismāīl Khān, Pakistan
- Samina International Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Young cigarette smokers (10 cigarette/day for at least 10 years)
- Male
- Age 25-45 years
- Sedentary lifestyle
- Body mass: less than 80kg
- BMI:22-30
Exclusion Criteria:
- Heart or pulmonary disease
- MSK disorder
- incapable of realizing the protocol of exercises,
- Recent surgery
- Recent Trauma.
- Any infective respiratory illness.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: lower limb strength training
Experimental group will receive lower limb strength training
|
Experimental group will receive lower limb strength training treatment for three days a week and each session will last for an hour for 3 consecutivemonths.
Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.
|
|
Other: endurance training
control group will receive endurance training.
|
Control group will receive endurance training, treatment for three days a week and each session will last for an hour for 3 consecutivemonths.
Measurement will be recorder pre-treatment and post treatment of both groupsat baseline,3rd, and 6th week.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Spirometry
Time Frame: 6 weeks
|
Spirometry is one of the Pulmonary Function Test; they are useful investigations in the management of patients with respiratory disease or respiratory weakness secondary to neurological impairment.
They aid diagnosis, help monitor response to treatment and can guide decisions regarding further treatment and intervention.
Spirometry can measure all the lung volumes except residual volume.
|
6 weeks
|
|
International Physical Activity Questionnaire
Time Frame: 6 weeks
|
The International Physical Activity Questionnaire is a 27-item self-reported measure of physical activity for use with individual adult patients aged 15 to 69 years old.
The International Physical Activity Questionnaire can be used clinically and in population research that compares physical activity levels between populations internationally.To calculate MET minutes a week multiply the MET value given (remember walking = 3.3, moderate activity = 4, vigorous activity = 8) by the minutes the activity was carried out and again by the number of days that that activity was undertaken.
For example if someone reports walking for 30 minutes 5 days a week then the total MET minutes for that activity are 3.3 X 30 X 5=495 Met minutes a week.
|
6 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Maria Razzaq, MsCPPT, Riphah International University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2023
Primary Completion (Actual)
July 15, 2024
Study Completion (Actual)
July 18, 2024
Study Registration Dates
First Submitted
August 13, 2024
First Submitted That Met QC Criteria
November 3, 2024
First Posted (Estimated)
November 5, 2024
Study Record Updates
Last Update Posted (Estimated)
November 5, 2024
Last Update Submitted That Met QC Criteria
November 3, 2024
Last Verified
November 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- Masroor Alam
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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